Weekly first-line chemotherapy of metastatic breast cancer with cyclophosphamide and epirubicin

Tumori. 1992 Oct 31;78(5):338-40. doi: 10.1177/030089169207800510.

Abstract

Forty-six patients with metastatic breast cancer who had not received previous chemotherapy for advanced disease entered a phase II trial of weekly chemotherapy with cyclophosphamide (250 mg/m2) + epirubicin (25 mg/m2) for 16 weeks. The overall response rate was 61% (95% confidence limits, 47-75%), with 10 complete and 17 partial responses. Toxicity was mild and confined to nausea and vomiting and asymptomatic neutropenia (except in 2 cases). Sixty-three per cent of patients had no side effects. Weekly cyclophosphamide + epirubicin is an active and nontoxic regimen for patients with metastatic breast cancer who have had no prior anthracycline-containing adjuvant chemotherapy.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase II

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / secondary
  • Cyclophosphamide / administration & dosage
  • Drug Administration Schedule
  • Epirubicin / administration & dosage
  • Female
  • Humans
  • Middle Aged
  • Time Factors

Substances

  • Epirubicin
  • Cyclophosphamide